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Comparing Postoperative Pain After Vessel Sealing Device Versus Conventional Suturing Methods for Vaginal Hysterectomy and Pelvic Reconstructive Surgery

NCT05192954 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 95

Last updated 2024-11-22

No results posted yet for this study

Summary

This study will investigate pain outcomes for patients undergoing vaginal hysterectomy with pelvic reconstructive surgery using the LigasureTM vessel sealing device as compared to conventional clamping and suturing methods.

Conditions

  • Pelvic Organ Prolapse

Interventions

DEVICE

LigaSureTM vessel sealing device

Device will be used to clamp, cauterize, seal, and transect tissue during vaginal hysterectomy.

Sponsors & Collaborators

  • TriHealth Hatton Research Institute

    collaborator OTHER

  • Marlana McDowell

    lead OTHER

Principal Investigators

  • Jennifer Yeung, DO · TriHealth Inc.

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
SINGLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Max Age
80 Years
Sex
FEMALE
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2022-01-28
Primary Completion
2023-12-30
Completion
2024-10-28
FDA Device
Yes

Countries

  • United States

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT05192954 on ClinicalTrials.gov